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Product Preference With Systane Compared to Artificial Tears on Frequency of Drop Use

NCT00347984 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2012-04-10

No results posted yet for this study

Summary

The objective of this study was to evaluate the effect of Systane® compared to marketed artificial tears on the frequency of drop use.

Conditions

  • Dry Eye

Interventions

OTHER

Systane Lubricant eye drops

Sponsors & Collaborators

  • ORA, Inc.

    collaborator INDUSTRY

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Mike Christensen · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-12-31
Primary Completion
2006-02-28
Completion
2006-02-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00347984 on ClinicalTrials.gov